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  2. Zellweger syndrome - Wikipedia

    en.wikipedia.org/wiki/Zellweger_syndrome

    Zellweger syndrome is a rare congenital disorder characterized by the reduction or absence of functional peroxisomes in the cells of an individual. [1] It is one of a family of disorders called Zellweger spectrum disorders which are leukodystrophies .

  3. Zellweger spectrum disorders - Wikipedia

    en.wikipedia.org/wiki/Zellweger_spectrum_disorders

    Zellweger spectrum disorders are a group of rare disorders that create the same disease process. [1] The subdivisions of this spectrum are hyperpipecolic acidemia , infantile Refsum disease , neonatal adrenoleukodystrophy , and Zellweger syndrome .

  4. List of abbreviations for diseases and disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_abbreviations_for...

    XLP syndrome X-linked lymphoproliferative syndrome (see Duncan Disease) XLSA X-linked sideroblastic anemia: XMEA X-linked myopathy with excessive autophagy: XMEN X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia XP Xeroderma pigmentosa: XSCID X-linked severe combined immunodeficiency: XXX syndrome ...

  5. Plasmalogen - Wikipedia

    en.wikipedia.org/wiki/Plasmalogen

    There is some evidence from humans and animals that there are reduced levels of plasmalogens in the brain in neurodegenerative disorders including Alzheimer disease, Parkinson's disease, Niemann–Pick disease, type C, Down syndrome, and multiple sclerosis, it is not clear if this is causal or correlative. [20]

  6. D-bifunctional protein deficiency - Wikipedia

    en.wikipedia.org/wiki/D-bifunctional_protein...

    Peroxisomes contain many different enzymes, such as catalase, and their main function is to neutralize free radicals and detoxify drugs. For this reason peroxisomes are ubiquitous in the liver and kidney. D-BP deficiency is the most severe peroxisomal disorder, [1] often resembling Zellweger syndrome. [2]

  7. Infantile Refsum disease - Wikipedia

    en.wikipedia.org/wiki/Infantile_Refsum_disease

    Infantile Refsum disease (IRD) is a rare autosomal recessive [2] congenital peroxisomal biogenesis disorder within the Zellweger spectrum.These are disorders of the peroxisomes that are clinically similar to Zellweger syndrome and associated with mutations in the PEX family of genes.

  8. Neonatal adrenoleukodystrophy - Wikipedia

    en.wikipedia.org/wiki/Neonatal_adrenoleukodystrophy

    It is part of the Zellweger spectrum. It has been linked with multiple genes (at least five) associated with peroxisome biogenesis and has an autosomal recessive pattern of inheritance. [ 2 ]

  9. List of diseases (Z) - Wikipedia

    en.wikipedia.org/wiki/List_of_diseases_(Z)

    Zadik–Barak–Levin syndrome; ZAP70 deficiency; Zamzam–Sheriff–Phillips syndrome; Zechi-Ceide syndrome; Zellweger syndrome; Zenker's diverticulum; Zieve's syndrome; Zika Virus; Zimmerman–Laband syndrome; Zinc deficiency; Zinc toxicity; Zlotogora syndrome; Zollinger–Ellison syndrome; Zonular cataract and nystagmus; Zori–Stalker ...